Bacterial capsules: Occurrence, mechanism, and function

In environments characterized by extended multi-stress conditions, pathogens develop a variety of immune escape mechanisms to enhance their ability to infect the host. The capsules, polymers that bacteria secrete near their cell wall, participates in numerous bacterial life processes and plays a crucial role in resisting host immune attacks and adapting to their niche. Here, we discuss the relationship between capsules and bacterial virulence, summarizing the molecular mechanisms of capsular regulation and pathogenesis to provide new insights into the research on the pathogenesis of pathogenic bacteria.

In environments characterized by extended multi-stress conditions, pathogens develop a variety of immune escape mechanisms to enhance their ability to infect the host.The capsules, polymers that bacteria secrete near their cell wall, participates in numerous bacterial life processes and plays a crucial role in resisting host immune attacks and adapting to their niche.Here, we discuss the relationship between capsules and bacterial virulence, summarizing the molecular mechanisms of capsular regulation and pathogenesis to provide new insights into the research on the pathogenesis of pathogenic bacteria.
In bacteria, polymers known as capsules are generated at the periphery of the cell wall, enveloping the entire cell.Capsules connect to the peptidoglycan in Gram-negative bacteria or the plasma membrane in Gram-positive bacteria via covalent attachments to either phospholipid or lipid-A molecules.Capsules may also establish direct connections with surface proteins on the bacterial membrane 1 .For most bacteria, capsules primarily consist of polysaccharides, exemplified by Streptococcus suis (S. suis) 2 .Some capsules primarily consist of polypeptides, as in Bacillus anthracis 3 , while others, like Bacillus megaterium 4 , contain both polysaccharides and polypeptides.Capsular polysaccharides (CPS) were initially described as "halo" by Pasteur in 1881.CPS was isolated and discovered by Avery and Dochez in 1917 5 .It was not until 1925 that Avery elucidated the carbohydrate nature of the substance in the microbial capsule 6 .Capsules are prevalent in natural pathogens and participate in various bacterial cellular processes.Capsules regulate the size and dispersion of bacterial biofilm, contributing to sustained infections within hosts 7 , reducing the efficacy of antimicrobial peptides and complement 8 , suppressing phagocytosis by innate immune cells, promoting intracellular survival 7,9 , and aiding in defence against antimicrobial agents 10 .In this review, we summarize the role of capsules in bacterial virulence and analyze their regulation mechanisms.

Capsules biosynthesis
Capsules primarily consist of high molecular weight polysaccharides, which are essentially oligosaccharide repeating units.However, some bacterial capsules are atypical: the capsule of Yersinia pestis is a protein polymer composed of 17-kDa subunits 11,12 , and the capsule of Bacillus anthracis consists of D-glutamic acid 13 .Additionally, the O-antigen capsule and the capsule-like complex (CLC) are identified as capsules of Francisella tularensis (F.tularensis) 14 .The O-antigen capsule is composed of mannose, rhamnose, and dideoxy sugars, whereas the CLC comprises proteins and carbohydrates 15 .However, the precise role these capsules play in the virulence of F. tularensis remain to be fully elucidated.Further research is required to clarify the structure and contributions of each capsule to the pathogenesis and virulence of F. tularensis.
Currently, three primary capsule synthesis pathways are recognized: the Wzx/Wzy-dependent mechanism, the ATP-binding cassette (ABC) transporter-dependent mechanism, and the synthase-dependent mechanism 16,17 .Over 90% of S. pneumoniae serotypes synthesize capsules via the Wzx/Wzy-dependent mechanism, characterized by the formation of repeat units and nonprocessive polymerization 18 .This mechanism is also fundamental to the synthesis of group I and group IV capsules in Gramnegative bacteria 19 .The initial step involves transferring a 1-phosphate to the lipid carrier (undecyl isoprene phosphate) on the cell membrane's cytoplasmic surface.Following this, the complete repeat unit is turned outward by the Wzx flip enzyme, and the Wzy polymerase attaches the growing polymer chain to the newly formed repeat unit (Fig. 1, a, b) 19 .In S. pneumoniae serotypes, both with and without glucose (Glc), this step is accomplished by liposome and Glc-1-phosphotransferase (Glc-1-P) CpsE/ WchA and CPS site transferase from Wcil, WcjG or WcjH homologous groups, respectively 20 .Group II and group III capsules are called ABCdependent capsule.In this pathway, new polysaccharide chains undergo polymerization in the cytoplasm and are associated with phospholipid receptors.These chains are then transported across the intima by ABC transporters (Fig. 1c).Even with these variations, both Wzx/Wzy and ABC- dependent mechanisms employ similar outer membrane proteins belonging to the polysaccharide export family for the transportation of capsules across the bacteria's outer membrane 16 .For group IV capsules, CPS synthesis relies on Wzy polymerase and does not involve the Wzx flip enzyme.Additionally, CPS synthesis can occur via the synthase-dependent mechanism, wherein specific enzymes are responsible for initiating, polymerizing, and translocating the capsules (Fig. 1, d, e) 21 .For instance, S. pneumoniae serotype 3 and 37 utilize a single enzyme mechanism, which initiates capsule synthesis by transferring sugar to lipid receptors and subsequently adding additional sugars for extension 22 .However, it remains a puzzle why the Wzx/Wzy-dependent mechanism predominates in most Gram-positive bacteria, while the synthase-dependent mechanism is less common 23 .
The initial identification of protein capsules occurred in Bacillus anthracis 24,25 , and subsequent elucidation of their biosynthetic pathways was achieved in Bacillus licheniformis 26 .In the absence of hydroxylamine, γ-Lglutamyl adenylate residue forms, which is then converted to γ-D-glutamyl adenylate residue upon activation.A protein-bound thioester (S-protein) may serve as a second intermediate in this process 27 .The final step involves transferring the activated glutamate to an endogenous membrane-bound poly (γ-D-glutamyl) acceptor.Consequently, polyglutamyl chain extension occurs by adding new glutamyl units to the terminal amino group of the receptor-bound glutamyl residue (Fig, 1f).In summary, gaps remain in understanding protein capsule synthesis and assembly, particularly regarding specific molecular mechanisms, such as the completed polypeptide chain outside the membrane.

Serotypes and pathogenicity
Capsule types are influenced by various factors, including the number and sequence of monosaccharide components, the position of glycosidic linkages, the configuration (L or D) of components, and the degree of chemical modification, such as O-acetylation.Consequently, capsular structures are diverse, including hyaluronic acid (HA) 28 , heparosan 29 , chondroitin 30 , polysialic acid (PSA) 31 , and colanic acid 32,33 .The composition of the capsules facilitates further differentiation of bacteria into distinct groups (serotypes, serovars).Escherichia coli (E.coli) produces approximately 80 distinct capsule types, which were further categorized into four major groups: Group I, Group II, Group III, and Group IV, including the PSA-containing K1 capsule, chondroitin-containing K4 capsule, and heparosan-containing K5 capsule (Fig. 2A) 34 .Colanic acid is a capsule whose structure is similar to the group I capsule.Its biosynthesis occurs via the Wzx/Wzy-dependent pathway as in the the group I capsule 35 .A notable distinction is that E. coli cultured in laboratory conditions at 37 °C does not produce colanic acid 36 .In S. pneumoniae, 93 capsular serotypes have been identified, most of which are capable of causing infection 18,[37][38][39] .S. pneumoniae primarily synthesized its CPS in trisaccharide units, though variations exist among serotypes.For serotype 12 F, CPS synthesis is based on hexasaccharides 40 .In serotype 4, CPS comprises a tetrasaccharide repeating unit with pyruvate modifications (Fig. 2B) 41 .Serotype 6 A' CPS, based on tetrasaccharides, includes a rhamnose modification 42 .Streptococcus suis (S. suis) strains were initially classified into 35 serotypes based on CPS antigenicity [43][44][45] , later revised to 33 serotypes 46 .
Significant variation in capsule structure exists between different bacteria and among serotypes within the same species, contributing to diverse virulence (Table 1).Specific S. pneumoniae serotypes (1, 4, 5, 8, 12F, 18C and 19A) are highly invasive, while others (6A, 6B, 11A, and 23F) are reported to be less aggressive [47][48][49][50] .In S. aureus, serotypes 5 and 8, out of 11 known serotypes, are predominantly responsible for human infections 51 .The polysaccharides of serotypes 5 and 8 differ only in sugar linkages and O-acetylation sites of the mannosaminuronic acid residues (Fig. 2B) 52,53 .In Haemophilus influenzae (H influenzae), the capsules composed of polyribose ribitol phosphate connected by phosphodiester bonds render serotype b (Hib) the most virulent, followed by serotype a (Hia) and other capsular types 54 .Streptococcus pyogenes (GAS) groups A-C causing pharyngitis are typically not associated with skin infections (group D), and the opposite is also true, although certain serotypes show no particular tissue preference (group E) 55,56 .Considering these observations, researchers speculate that capsule virulence may be correlated with the frequency of monomer repetition or the specific type of monomer.In a mouse infection model, highly virulent serotypes of Klebsiella pneumoniae (K.pneumoniae), notably K2, which is associated with bacteremia, are devoid of the mannoseα-2/3-mannose structure that present in less virulent strains 57,58 .
Capsular switching is common in bacterial populations, exemplified by S. pneumoniae serotypes 11A and 11E.Serotype 11E, while rare in nasopharyngeal (NP) isolates, is frequently found in invasive pneumococcal disease (IPD) isolates 59 .Serotype 11E is identical to 11A, except that wcjE is inactivated, resulting in a lack of binding to ficolin-2 60,61 .In addition, most serotype 11E isolates possess wcjE mutations, including missense and nonsense mutations, single-base insertions and deletions, as well as transposon insertions 61 .This indicates that serotype 11A evolves into serotype 11E within populations, facilitating escape from ficolin-2-mediated phagocytosis during invasive S. pneumoniae infections.Similarly, the distinction between serotypes 9V and 9A lies solely in wcjE mutations, with the inactivation supporting the evolution from 9V to 9A 62,63 .Frequent variations through homologous recombination and horizontal gene transfer result in numerous uncharacterized components within capsular systems, including genetic components, proteins, or other molecular structures 64 .As a result, only a limited number of studies have reported on the frequency and diversity of capsules.To address this, Rendueles et al. developed protein profile models for identifying key components of various capsule biosynthetic pathways 65 .Wick et al. introduced Kaptive Web, an online tool for rapidly typing Klebsiella's K and O loci 66,67 .This method was also applied to identify Acinetobacter baumannii (A.baumannii)'s KL and OCL loci 68 .These developments offer significant technical support for identifying prokaryotic capsules.

Biological functions and pathogenicity of capsules
Adherence Capsules facilitate bacterial adhesion to surfaces and other bacteria, enhancing colonization in diverse niches and fostering biofilm formation.The bacterial biofilm matrix consists of polysaccharides and is enriched with extracellular proteins and various small molecules, including extracellular DNA (eDNA) 69 .Eliminating the frwC gene, encoding a hypothetical fructose-specific enzyme II C, can stimulate magA (also known as wzy, encoding a polymerase essential for capsule synthesis) transcription, thus enhancing CPS production and in vitro biofilm formation in K. pneumoniae 70 .Self-phosphorylating Wza proteins facilitate CPS assembly.The absence of wza impairs CPS transport to the outer membrane and its fixation, markedly diminishing cell adhesion in A. baumannii and leading to in vitro biofilm defects 71 .There is also a mechanism different from the "classic" static biofilm formation.During periods of high CPS expression, floating S. pyogenes aggregates connect via CPS to facilitate in vitro biofilm formation (Fig. 3A, a).However, the "classic" mechanism can overshadow this biofilm formation mechanism 72 .Biofilm resulting from bacterial attachment can have far-reaching effects.For example, the biofilm formation of retention tubes in inpatients will cause more severe nosocomial infections 73 .The Pseudomonas aeruginosa biofilm in patients with cystic fibrosis forms a permeable barrier that can resist the function of antibiotics 74 .
Nevertheless, the impact of capsules on bacterial adhesion remains a subject of debate.An alternative perspective posits that capsules formation primarily occurs during the mature stage of bacterial biofilm, where CPS secretion facilitates biofilm dissociation (Fig. 3A, a), enabling bacterial dispersion and subsequent biofilm development 7 .This effect could be due to the masking of adhesive proteins on the bacterial surface or the capsule's physical and chemical properties.Antigen 43 (Ag43), a surface protein facilitating cell-to-cell aggregation 75 , is hindered in its function when a K1 or K5 capsule is expressed, as the extended polysaccharides sterically block adhesion 76 .Likewise, CPS production can obscure ClfA (Clumping Factor  19 ; Pasteurella multocida (A, B) 207 ; Neisseria meningitidis (B, W) 132 ; Klebsiella pneumoniae (K1, K2) 208,209  A) on the cell wall, thereby reducing S. aureus's capacity to adhere to platelets 77 .Additionally, certain studies indicate that capsules may negatively regulate initial in vitro biofilm formation.The negative charge carried by CPS is thought to hinder early bacterial accumulation, consequently inhibiting in vitro biofilm formation 78 .This phenomenon, far from being accidental, has garnered attention since the early 21st century, with the capsule's biological properties considered promising for medical surface coatings.Group II capsules extract of E. coli can induce a significant charge reversal at latex particles' interface ζ (zeta) potential, resulting in a highly anionic nature 79 .Besides electrostatic modifications, active supernatants can also remodel colloid surface properties, potentially involving surface hydration and steric repulsion.Consequently, Group II capsules significantly reduce biofilm formation on glass surfaces by E. coli and various Gram-positive and Gram-negative pathogens, primarily by weakening cellsurface contacts and reducing cell-cell interactions (Fig. 3A, b).
The influence of capsule serotypes on in vitro biofilm varies.In Bacteroides thetaiotaomicron biofilm grown in a chemostat for 8 days, CPS 8 expression was upregulated, whereas capsules 1, 3, 4, and 6 showed downregulated 80 .However, there is no evidence that increased in vitro adhesion correlates with improved colonization in axenic mice, indicating that enhanced in vitro biofilm formation may not predict in vivo colonization capacity 81 .Capsules-mediated bacterial adhesion is also linked to the bacterial growth cycle.S. aureus exhibits stronger adhesion to human endothelial cells (EC) during the exponential growth phase compared to the stationary phase 82 .Ashbaugh et al. conducted comparative experiments with primate models and revealed that CPS-free mutants were eliminated from the baboon pharynx more rapidly than wild-type strains in short-term colonization studies 83 .In long-term carrier models, it was observed that carriage isolates developed mutations leading to reduced or absent hyaluronic acid production, suggesting that CPS enhances transmission and initial colonization.Additionally, the late downregulation or loss of CPS synthesis may aid in the long-term survival of the strain in vivo 84 .

Resistance to host immunity
In invasive bacterial infections, the capsule's interaction with the host immune system is pivotal in determining infection outcomes 85 .Capsules confer resistance to nonspecific host defense mechanisms, particularly without specific antibodies.Such mechanisms involve the activation of the complement cascade and C3b-mediated neutrophil phagocytosis via alternative pathways.Activation of the alternative pathway occurs via the nonspecific attachment of the serum protein C3b to the bacterial surface.Upon attachment, C3b engages with factor B, forming C3 convertase (C3bBb).This leads to enhanced C3 attachment and the development of a membrane attack complex (MAC) on the bacterial surface, culminating in lysis and the demise of the bacteria 86 .CPS impedes the binding of immunoglobulin G (IgG) to bacteria by masking antigen-binding sites on the bacterial surface and diminishes the effect of C3b/iC3b by obstructing the conversion of C3b to iC3b on the bacterial surface (Fig. 3B, a) 87 .CPS that contains N-acetylneuraminic acid do not initiate the alternative pathway.The inhibition of this pathway can be ascribed to the direct interaction of N-acetylneuraminic acid in polysaccharides with factor H. The bound factor H serves as a cofactor, initiating the combination of factor I and C3b to form iC3b, thus preventing MAC formation 88 .The capsule collaborates with cell surface structures like O antigen to resist complement-mediated killing.Consequently, this specific combination exhibited by the bacteria confers significant resistance to complement-mediated killing 89 .Additionally, CPS can counteract complement-mediated opsonophagocytosis.The capsules mask C3b on the inner cell surface, thereby preventing its binding to the C3b receptor (e.g., CR1) on the phagocyte surface 90,91 .Hurst et al. noted in their immunohistochemical study of a mouse infection model that neutrophils infiltrated the core of GAS infections, irrespective of HA capsule expression.Within 24 h post-infection, there was an upsurge in the neutrophil population (GR1+), and strains with capsular defects were rapidly eliminated by 48 h.Moreover, this does not lead to nasopharyngeal restructuring conducive to favorable inflammation.Furthermore, capsules may play a role in  pathogenesis by preventing the entrapment of S. pneumoniae in neutrophil extracellular traps 92 .
Beyond passive responses to the host immune system, bacterial capsules actively modulate host immune responses by directly influencing cytokine release and disrupting the coordination of host cell-mediated immune responses 93 .For instance, the capsule of Francisella tularensis (F.tularensis) can impede the R848-induced increase in lactic acid secretion.This inhibition subsequently impedes phagocyte metabolic transition from oxidative phosphorylation to glycolysis, ultimately suppressing cytokine secretion 94 (Fig. 3B, b).However, the mechanism of action of the capsules is still unclear, and the capsules' direct mediation of immune cell responses remains to be explored.

Niche adaptation
Capsules frequently constitute the outermost layer of cells and facilitate direct interaction between bacteria and their environment, thus influencing bacterial adaptation to new niches.Species encoding capsule, particularly environmental bacteria and facultative pathogens with multiple capsule genes, exhibit higher levels of genetic diversification than their counterparts, contributing to broader environmental adaptability 95 .
During the invasion of a host by pathogenic bacteria, these organisms encounter significant environmental changes, including low pH, elevated temperature, reduced oxygen pressure, and altered osmotic pressure.When pathogenic bacteria invade the epithelial barrier and enter the bloodstream, they are exposed to a 0.15 M sodium chloride osmotic pressure, triggering prioritized CPS synthesis 96 .Upon entering the bloodstream and invading deeper tissues and organs, bacteria encounter the challenge of low oxygen pressure in these environments.In S. pneumoniae, CPS synthesis is reduced under hyperoxic conditions compared to hypoxic growth, a phenomenon linked to CpsB phosphatase activity, not CpsD phosphorylation levels 97 .Considering S. pneumoniae's growth environment, its benign colonization in high-oxygen nasopharyngeal areas leads to decreased capsule synthesis.Upon transfer to host defense sites with lower oxygen levels, an increase in capsule synthesis is observed 18 .A similar phenomenon is observed in S. aureus, where capsule synthesis in three serotypes is inhibited in environments supplemented with 1%-5% CO 2

98
. Further research indicated that CO 2 impedes the transcription of the cap gene 99 .However, it is important to note that higher oxygen concentrations are not more beneficial.In S. pneumoniae, high oxygen concentrations regulate CpsB phosphatase activity, inhibiting CpsD phosphorylation.Impaired CPS regulation due to tyrosine phosphorylation in CpsD affects S. pneumoniae's capacity to transition from the lungs to the bloodstream 100 .Furthermore, factors such as iron-limited culture 101 , acidic conditions 102,103 , and the nutrient richness 104 of the environment also play crucial roles in capsule synthesis.
The influence of capsules presence on bacterial adaptation and its role in strain evolution were not empirically confirmed until Nucci et al. conducted the first relevant evolutionary study 105 .In an evolutionary experiment spanning 675 generations (102 days) with three phylogenetically distant strains of K. pneumoniae, Nucci et al. discovered that both capsulated and non-capsulated populations possessed a competitive edge over their progenitor strains, with average fitness increases of 58% and 36%, respectively.This finding suggests that capsules play a significant role in enhancing the average fitness of populations 105 .The presence of capsules in adapting populations influences phenotypic changes significantly.Evolved capsulated bacteria exhibit an increase in or the emergence of a hypermucoidy phenotype (HMP), while non-capsulated populations adapt through higher population yields, enhanced surface polysaccharides, and biofilm formation 105 .The competitive advantage of the HMP has been demonstrated in bacteria and fungi, with HMP preventing predation by amoeba or bacteria on Klebsiella 106,107 .Cryptococcus neoformans develops resistance to amoeba by increasing its capsules size 108 .Furthermore, E. coli exhibits increased mucoidy when interacting with macrophages or predatory bacteria, suggesting that this phenotype is advantageous outside the host 109,110 .The research by Nucci et al. suggests that capsulated and non-capsulated populations adapt to niches via distinct pathways.Capsulated strains frequently demonstrate genetic mutations that directly impact capsule synthesis 105 .So, how do non-capsulated cells adapt to the new environment?Firstly, non-capsulated strains adapt through increased production of alternative extracellular polysaccharides on the cell surface, facilitated by Wzi (a functional lectin-binding protein), thereby mimicking capsule functionality 111,112 .Secondly, most non-capsulated clones accumulate mutations in the capsule's regulatory elements, reducing in the expression cost of other genes within the operon 113 .This reduction in capsule expression may confer an advantage when capsules are regained through horizontal gene transfer.Furthermore, this can result in capsule swapping, expressing a novel serotype with a different biochemical composition among strains with similar chemical compositions 113,114 .Ultimately, the coadaptation of bacterial populations, both encapsulated and non-encapsulated, leads to a more complex population structure and an increase in cellular interactions 115,116 .

Other functions
Capsules are known for their contribution to bacterial adhesion and antiphagocytosis, so these two properties have been most widely studied.With the increasingly in-depth study of capsules, other virulence potentials have gained attention.
Presently, the mortality and morbidity rates linked to bacterial meningitis remain alarmingly high.Earlier studies have reported capsules' role in enabling bacteria to breach the blood-brain barrier (BBB).E. coli with the K1 CPS is particularly prominent among isolates that cause neonatal meningitis.Investigations have revealed that microbial elements, including the K1 capsule, are crucial for the invasiveness of E. coli.The K1-cps locus is present in a quarter of bloodstream infection isolates and has independently emerged in at least four ExPEC phylogroups over the last 500 years 34 .Furthermore, the K1 capsule aids in the invasion of brain microvascular endothelial cells (BMEC) by E. coli 117 .Unlike other meningitis-causing bacteria like Group B Streptococci (GBS) 118 , E. coli K1's invasion does not compromise the integrity of the cell monolayer structure.E. coli K1 invades BMEC via a zipper-like mechanism and travels through enclosed vacuoles 119 .Employing a reverse-oriented Transwell filter system with porcine choroid plexus epithelial cells (PCPEC), Tenenbaum et al. explored the process of bacterial invasion and movement from the basolateral (blood) aspect to the apical (cerebrospinal fluid) aspect, a novel approach in this field.Their findings suggest that S. suis translocation through PCPEC could be regulated by capsule-derived signals dependent on the lipid kinase phosphatidylinositol 3-kinase pathway (Fig. 3C) 120 .However, there exist conflicting research findings indicating that capsular presence may in fact attenuate bacterial virulence.According to Gendrin et al., GBS strains enhance their intracellular survival and propagation by abandoning their capsule.This mechanism does not involve concealment within macrophages (also called the "Trojan horse" mechanism 121,122 ).Concurrently, there is an observed increase in the permeability of the BBB associated with GBS 123 .
The contribution of capsules to bacterial drug resistance is welldocumented in scientific literature.In A. baumannii, antibiotics induce stress, leading to increased transcription of the K locus genes (responsible for capsule biosynthesis) via the BfmRS two-component regulatory system 124 .This sequence of events triggers capsule synthesis, which confers resistance to chloramphenicol and erythromycin (Fig. 3D, a).In High-alcoholproducing K. pneumoniae (HiAlc Kpn), glucose inhibits the expression of crp and enhances CPS production, thereby increasing the strain's drug resistance 125 .Furthermore, several studies have demonstrated that externally added capsules can bind antimicrobial peptides (AMPs), potentially blocking their entry into the cell and diminishing the efficacy of polymyxin (Fig. 3D, b) 126,127 .When the capsule functions naturally, attached to the outer membrane, it increases antimicrobials' concentration near the cell (Fig. 3D, c) 128 .This elevated concentration of antimicrobial peptides benefits agents like colistin, which disrupt the outer cell membrane and induce cell lysis by binding to lipopolysaccharides and phospholipids 129  GBS 123 .Given the limited research, the contribution of the capsule to bacterial antibiotic resistance persists as a debated topic, and the investigation into whether this role is specific to particular antibiotic species remains imperative.

Regulation mechanisms
Two-component systems regulate capsules Two-component systems (TCS) represent a predominant mechanism in bacterial signal transduction 130 .In bacteria, TCS plays a pivotal role in gene regulation, responding to environmental changes.These protein families are implicated in adapting to diverse stress conditions and in essential cellular pathways 131 .
The cps locus promoter in Neisseria meningitidis is situated in the intergenic region between biosynthesis and the conserved envelope transport operon.The MisR/MisS TCS negatively regulates CPS production by directly binding to the promoter region (Fig. 4A) 132 .In GAS, the CsrRS TCS as a regulator of capsule production.This system comprises the loci csrR and csrS (also known as covR and covS) 133 .While the inactivation of csrR did not alter M protein expression or hemolytic activity, it resulted in a sixfold increase in capsule production, whereas subsequent studies showed that the system influences the expression of additional virulence factors, including streptokinase (ska), mitogenic factor (speMF) and cysteine protease (speB) 28 .The RstAB TCS positively regulates CPS synthesis, aiding Photobacterium damselae in evading fish host cells' defense 134 .ArlR directly activates the TCS often regulates capsule biosynthesis by directly binding to the promoters of capsule synthesis genes, thereby responding to environmental changes.The ArlRS TCS of S. aureus can directly activate the global transcription factors MgrA and Spx expression, thereby regulating capsule synthesis and antibiotic resistance.N. meningitidis MisR/MisS TCS can negatively regulate the production of CPS by directly binding to the region.B QS regulation of capsule synthesis.AI-2 regulates the phosphotransferase system on the membrane surface to limit the intake of galactose, ultimately affecting the synthesis of CPS.C Metabolic regulation of capsule synthesis.The synthesis of bacterial capsule is related to the fate of pyruvate.
Pyruvate is converted into acetyl-CoA and enters the TCA cycle, which is beneficial to capsule synthesis.Therefore, inhibiting the conversion of pyruvate to lactic acid can promote the synthesis of bacterial capsule.In addition, excessive xylitol intake will stimulate the phosphotransferase system on the cell membrane, and phosphorylated xylitol impairs capsule synthesis and ultimately affects bacterial adhesion.D External environmental conditions promote Stk1/Stp1 system phosphorylate CcpS, thus relieving the inhibition of CcpS on CpsB.CpsB assists the dephosphorylation of phosphorylated CpsD (CpsD-P).expression of global transcription factors MgrA and Spx in S. aureus 135 (Fig. 4A), influencing capsule synthesis genes, wall-anchored adhesins (ebh, sdrD), cell wall remodeling genes (lytN, ddh) and anaerobic metabolism genes (adhE, pflA, nrdDG).This activation promotes capsule synthesis and impacts the TrfA protein, a component of the Clp proteasome complex, which plays a role in resisting cell wall-targeting antibiotics, thereby enhancing antibiotic resistance 136,137 .
In summary, most TCS are recognized as key molecular mechanisms regulating bacterial capsule synthesis, and the understanding of their interrelationships is becoming increasingly comprehensive.

Quorum sensing regulates capsules
Quorum sensing (QS) represents a form of inter-bacterial 'communication' 73 .In this process, bacteria synthesize and detect extracellular signaling molecules, termed auto-inducers (AI), leading to either the activation of regulatory proteins or the suppression of specific gene expression.This intricate system plays a crucial role in bacterial coordination and collective behavior.This process allows for the control of the physiological characteristics of microbial populations, including traits like motility, biofilm formation, immunosuppression, and nutrient utilization 138,139 .Studies have indicated that QS-regulated genes constitute 10% and 20% of the entire genome 140,141 .As research on QS deepens, more attention is being directed toward understanding the relationship between QS and capsules.
FruA, a fructose-specific phosphotransferase system component in S. pneumoniae, can sense AI-2.This sensing mechanism leads to the upregulation of the galactose ABC transporter and the Leloir pathway (Fig. 4B).Subsequently, it increases CPS synthesis, resulting in a high virulence phenotype 142 .Rgg/Shp144 and Rgg/Shp939 were proved to be another QS of S. pneumoniae by Zhi et al.The Rgg/Shp QS includes Rgg proteins (alternatively termed Gad or Mut), which are part of a conserved group of independent transcriptional regulators, and short hydrophobic peptides (Shp) 143,144 .Rgg/Shp1517 QS is necessary for S. pneumoniae to use galactose and mannose.However it is a negative regulator of capsular expression, which may involve binding Rgg to the capsular locus promoter (Fig. 4B) 145 .Additionally, the regulation of CPS by Rgg/Shp QS varies depending on the response to specific sugars.Rgg144 and Rgg939 were most significantly induced by mannose, followed by galactose, whereas Rgg1518 was primarily stimulated by galactose 146 .Furthermore, other quorum sensing systems have also been reported to be associated with capsule synthesis.For example, GtaR/I QS is involved in regulating Rhodobacter capsulatus (RcGTA) growth and capsules' formation, and the capsules also play a role in RcGTA adhesion as a receptor 147 .Agr (accessory gene regulator) QS positively regulates the production of type-5 capsular polysaccharide (CP5) in S. aureus, enhancing adhesion to inner epidermal cells (EC) 82 .

Metabolic activity regulates capsules
Capsules are crucial in bacterial invasive infections, acting as an energyconsuming virulence factor.Bacteria frequently utilize carbohydrates via glycolysis and other central carbon metabolism (CCM) to support the energy demands of capsule synthesis 104 .CCM encompasses enzymatic reactions converting carbon into energy, including glycolysis, the tricarboxylic acid (TCA) cycle, the gluconeogenesis, the pentose phosphate pathway (PPP), the glyoxylate shunt, the γ-aminobutyric acid (GABA) shunt, and the methylcitrate cycle 148 .As a central component of material metabolism, the TCA cycle plays an irreplaceable role in the life process of organisms.Pyruvate from glycolysis is converted to acetyl-CoA by pyruvate dehydrogenase, initiating the TCA cycle and providing energy for cells.Following the simultaneous deletion of spxB (pyruvate oxidase) and lctO (lactate dehydrogenase), acetyl-CoA and capsule production were restored in S. pneumoniae type 4, though the underlying mechanism remains elusive 149 .The prevailing hypothesis posits that the absence of lactate dehydrogenase leads to increased lactic acid levels, inhibiting lactate dehydrogenase activity.This inhibition facilitates bacterial capture of pyruvate, thus enhancing the conversion of pyruvate to acetyl-CoA (Fig. 4C).
Although S. aureus possesses pyruvate dehydrogenase, it directly converts pyruvate to acetic acid 150 .However, the impact of this conversion on acetyl-CoA and capsule synthesis remains unknown.Excessive sugar intake is deleterious, given that the glucose phosphotransferase system swiftly transports xylitol into cells and phosphorylates it, while the accumulation of excessive xylitol phosphate can exert toxic efforts on S. pneumoniae, impairing CPS production and diminishing adhesion to nasopharyngeal cells (Fig. 4C) 151 .CPS in S. aureus serotype 5 was eliminated in the presence of glucose, but this did not affect CPS synthesis in the ccpA (coding catabolite control protein A) deletion strain MST14 serotype 5. Seidl et al. found that cap operon expression in S. aureus serotype 5 was significantly lower compared to MST14, yet no prominent catabolite-responsive elements (CREs) were identified in the cap operon's genomic region, suggesting an indirect effect of CcpA on cap transcription 152 .
Additionally, a complex relationship exists between capsule types and metabolic cost.For instance, capsule exchange in S. pneumoniae may result in diminished fitness or viability, a consequence modulated by the carbon content and CPS charge of each polysaccharide 153 .Hathaway et al. compared growth phenotypes of S. pneumoniae across different capsular serotypes, finding that strains with a lower metabolic burden exhibited growth advantages 104 .Schipper et al. examined the impact of meningococcal CPS structure on the lethality of zebrafish embryos and neutrophil consumption post-infection.They observed a close relationship between the CPS structure and the carbon number in each polysaccharide repeat unit.Consequently, the variation in virulence among different capsule types may stem from metabolic cost differences rather than molecular interactions with host immune components 154 .

Other regulation mechanisms
Tyrosine phosphorylation, initially viewed as crucial in eukaryotic regulation 155 , is now recognized as a critical factor in bacterial physiology 156 .Although phosphorylation is a longstanding recognized posttranslational regulatory mechanism in bacteria, the significance of tyrosine phosphorylation was highlighted with the discovery of a tyrosine-phosphorylated protein in Acinetobacter johnsonii 157 .The cocci bacteria encode the first four genes, cpsABCD, in the cps locus, a sequence broadly conserved across species 18 .The cpsA gene encodes LytR-Cps2A-Psr (LCP) protein, which is believed to conjugate CPS to peptidoglycan (PG) 158 .The cpsB, cpsC, and cpsD genes form a tyrosine phosphoregulatory system controlling CPS assembly machinery 159,160 .CpsC is essential for CpsD's tyrosine phosphorylation.When CpsD self-phosphorylates (utilizing bound ATP), the resulting tyrosine phosphorylated CpsD (CpsD-p) dissociates from CpsC, reducing CPS production.CpsB assists in CpsD-p dephosphorylation, facilitating its interaction with CpsC, leading to an accelerated rate of CPS biosynthesis/polymerization 161,162 .The CpsBCD bacterial tyrosine kinase system responds to environmental changes (e.g., oxygen content 18 ), with the mechanism clarified by Tang et al.'s study in S. suis, enhancing understanding of the relationship between CpsBCD and signal transduction.CcpS, a protein regulating phosphatase CpsB's activity, links the Stk1/ Stp1 system (a serine/threonine kinase system controlling bacterial phosphosignaling) with the Wzx-Wzy pathway in bacteria.Stk1/Stp1 specially mediates Thr-phosphorylation of the CcpS protein.Non-phosphorylated CcpS can inhibit CpsB-catalyzed dephosphorylation of CpsD-P in vivo, leading to abnormal CPS synthesis in S. suis 163 (Fig. 4D).
The second messenger cyclic AMP (cAMP), small RNA, and ironacquisition systems are also found to be associated with capsule synthesis.Cyclic-3',5'-adenosine monophosphate (cAMP) is a ubiquitous second messenger, orchestrating essential processes in bacteria and eukaryotes 164 .K. pneumoniae regulates CPS production through cAMP-dependent carbon catabolite repression (CCR), enhancing protection from serum killing and phagocytosis and modifying oxidative stress resistance, improving phagosome survival 165 .In Vibrio parahaemolyticus, AI-2 QS controls the capsular synthesis and bacterial aggregation through self-inducing signals (S signals) affecting c-di-GMP levels 166 .Small RNAs (sRNAs), such as rss04 and rss03, are critical regulators of bacterial virulence, inhibiting CPS production after S. suis enters the brain, exacerbating the inflammatory response, and promoting meningitis 167 .The iron uptake system, a crucial regulatory mechanism in bacteria, has become a focal point of research.Bacteria stringently regulate iron transport and storage via Fur (ferric uptake regulator) to maintain iron homeostasis.Under iron-replete conditions, dimeric Fur complexed with Fe(II) binds to a 19 bp consensus DNA sequence in the promoters of iron uptake genes, inhibiting their transcription 168 .In K. pneumoniae, Fur suppresses CPS biosynthesis by inhibiting RmpA and RcsA.Interestingly, sRNA also plays a role in these regulatory activities 169 .sRNA RyhB activates the transcription of orf1 and orf16, components of the cps gene cluster open reading frames (ORFs)), independently of RmpA and RcsA 170 .However, since K. pneumoniae requires CPS for survival in the host, other positive regulatory systems responding to external iron influence CPS biosynthesis.IscR, a protein harboring a [2Fe-2S] cluster and encoded by the first gene of the iscRSUA operon 171 , orchestrates the regulation of genes engaged in diverse cellular processes that respond to environmental stimuli such as oxidative stress and iron 172 .With the [2Fe-2S] clusters, IscR's DNA binding specificity is broadened, enabling holo-IscR to interact with both type 1 and type 2 IscR box 173 , positively influencing CPS biosynthesis 174 .

Outlook
Given the substantial immunomodulatory characteristics of CPS, they have garnered considerable attention in vaccine development.Extensive research over the years has established the efficacy of vaccines based on polyvalent pneumococcal polysaccharides.This focus aligns with CPS's ability to modulate immune responses, underscoring its potential in preventive healthcare strategies.Mutagenesis-induced removal of CPS reveals antigenic cell wall proteins usually obscured by the dense capsular shell.The nonencapsulated mutant is anticipated to elicit a more potent immune response.Although the capsule's structural diversity, biosynthesis, and immunogenicity have been extensively studied, further research is required on their role in pathogen adhesion and regulatory mechanisms.Secondly, research on immune evasion predominantly centers on how capsules mask surface antigens of pathogenic bacteria.Studies on the capsule's active mediation of host immunity (e.g., F. tularensis 94 ) remain limited.Conducting further research will undoubtedly deepen our understanding of the capsule's biological functions and aid in developing treatment strategies.Additionally, bacteria can express multiple capsule types concurrently 65,175 .This capability of co-expression broadens the bacteria's range of environmental adaptabilities, including enhanced adhesion and virulence, thereby facilitating their ecological transition towards host colonization and pathogenesis 176 .Therefore, in the future, it is necessary to study in detail the mechanisms that lead to the acquisition of multiple capsules.

Fig. 1 |
Fig. 1 | Capsule synthesis mechanisms.Wzy-Dependent mechanism.The first three steps are universal: ①, phosphoglycosyltransferase (PGT) and serotype-specific glycosyltransferases (GT(s)) synthesize undecaprenyl diphosphate-linked oligosaccharide repeat units; ②, Wzx facilitates the translocation of these units across the membrane, followed by Wzy-mediated polymerization; ③, The phosphorylation cycle of Wzc, catalyzed by Wzb, is a crucial step.In Gram-positive bacteria (a): ④, The newly formed polymer is transferred onto a peptidoglycan assembly intermediate; ⑤, It gets anchored to the cell wall through LCP activity.In Gram-negative bacteria (b): ④, The polymer translocates across the outer membrane via Wza; ⑤, In some prototype and other species, Wzi assists in organizing the translocated polymer into surface-associated capsule structures.c ABC Transporter-Dependent mechanism.For Gram-negative bacteria, ①-② involve the assembly of sugar chains; ③, the ABC transporter (KpsMT) plays a pivotal role in exporting these chains; ④, KpsE and KpsD are essential for translocating the assembled chains across the periplasm and outer membrane.The specifics of the ABC-dependent pathway in Gram-positive bacteria remain unclear.Synthase-Dependent mechanism: ①, Initial synthesis of the short sugar chains; ②, Extension of these chains by glycosyltransferases.In Gram-positive bacteria (d): ③, Transfer of the polymer to the outer membrane.In Gram-negative bacteria (e): ③, Polymer translocation and anchoring to the cell wall via a translocation anchor.(f): Protein capsule synthesis pathway.The synthesis of the poly (y-D-glutamyl) capsule in Bacillus licheniformis involves a series of membrane-associated enzymatic reactions.Here, a polyglutamyl synthetase complex catalyzes the activation, racemization, and polymerization of L-glutamic acid, resulting in a high molecular weight polymer of y-D-glutamic acid.① L-Glu + ATP ⇌ γ-L-Glu-AMP + PPi; ② γ-L-Glu-AMP + S-protein⇌ γ-L-Glu-S-protein + AMP; γ-L-Glu-S-protein ⇌ γ-D-Glu-S-protein; ③, γ-D-Glu-S-protein + poly (γ-D-Glu) n → poly (γ-D-Glu) n+1 + S-protein.GT glycosyltransferase, LCP LytR-CpsA-Psr, OPX outer membrane polysaccharide, PCP polysaccharide copolymerase; PGT, phosphoglycosyltransferase, PHP polymerase and histidinol phosphatase, SA polysaccharide A, PTP phosphotyrosine phosphatase, Glu glutamate, S-protein a protein-bound thioester, as a second intermediate for the growing polymeric chains.

Fig. 3 |
Fig. 3 | The functions of capsule in the process of pathogenic bacterial infection.A The influence of capsules on bacterial adherence.(a) Capsules promote or inhibits the formation of bacterial biofilm.(b) The addition of exogenous CPS changes the physical properties of the surface of non-biological materials, make them carry high negative charge and inhibit the adhesion of bacteria.B Interfering with host immune responses.(a) S. pneumoniae masks body surface antigens through capsule to avoid phagocytosis by macrophages.(b) F.tularensis inhibits the metabolic transformation of phagocytes through the synthesis of capsules, and finally inhibits the secretion of cytokines.C Assisting bacterial BBB penetration.Bacteria break through the bloodbrain barrier by stimulating actin cytoskeleton rearrangement and various signal transduction pathways, including phosphatidylinositol-3-kinase (PI3K) and cytoplasmic phospholipase A2 (cPLA2).But at present, the effect on capsules is only phenotypic.D The impact of capsules on antibiotic resistance.(a) A. baumanii regulates the expression of K locus gene through the BfmRS TCS, which further promotes the synthesis of CPS and resists the killing of antibiotics, but the mechanism of CPS is still unknown.(b) Exogenous CPS adsorbs antimicrobial peptides (AMPs) and polymyxin, thus promoting the survival of bacteria.(c) The CPS located on the surface of bacteria adhere to polymyxin, which promotes the cleavage of polymyxin to the bacterial cell wall and finally promotes the death of bacteria.Positive regulation is indicated by red arrow, and negative regulation by blue arrow.

Fig. 4 |
Fig. 4 | Capsule regulation mechanisms.A TCS regulation of capsule synthesis.TCS often regulates capsule biosynthesis by directly binding to the promoters of capsule synthesis genes, thereby responding to environmental changes.The ArlRS TCS of S. aureus can directly activate the global transcription factors MgrA and Spx expression, thereby regulating capsule synthesis and antibiotic resistance.N. meningitidis MisR/MisS TCS can negatively regulate the production of CPS by directly binding to the region.B QS regulation of capsule synthesis.AI-2 regulates the phosphotransferase system on the membrane surface to limit the intake of galactose, ultimately affecting the synthesis of CPS.C Metabolic regulation of capsule synthesis.The synthesis of bacterial capsule is related to the fate of pyruvate.